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Chemical modification
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The purpose of the thesis is to synthesize the effective catalysts based on Pt/SBA-15 modifed with Al and/or B and their applicability in n-heptane hydroisomerization, tetralin hydrogenation and paracetamol detection.
129p
closefriend04
17-10-2021
20
4
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The aim of the thesis: Study on chemical constituents of two Knema species including Knema pachycarpa and Knema saxatilis growing in Vietnam. Evaluate cytotoxic and cetylcholinesterase enzyme inhibitory activitiesof isolates to find out bioactive compounds.
25p
extraenglish
24-05-2021
20
4
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The aim of the thesis: Study on chemical composition of starfish Acanthaster planci of Vietnam, synthesizing hydroxyl and oxime derivatives from a steroid isolated from this starfish and assessing biological activity of isolated and synthesized compounds.
26p
extraenglish
24-05-2021
24
4
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Study on chemical composition of starfish Acanthaster planci of Vietnam, synthesizing hydroxyl and oxime derivatives from a steroid isolated from this starfish and assessing biological activity of isolated and synthesized compounds.
26p
capheviahe26
25-01-2021
12
4
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The envelope protein gp64 of the baculovirusAutographa californicanuclear polyhedrosis virus is essential for viral entry into insect cells, as the glycoprotein bothmediates pH-dependentmembrane fusionandbinds tohost cell receptors. Surface modification of baculovirus particles by genetic engineering of gp64 has been demonstrated by various strategies and thus has become an important and powerful tool in molecular biology.
10p
research12
23-04-2013
28
2
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It was shown previously [Riedinger, H. J., van Betteraey-Nikoleit, M & Probst, H. (2002)Eur. J. Biochem.269, 2383–2393] that initiation ofin vivo SV40 DNA replication is reversibly suppressed by hypoxia in a state where viral minichromosomes exhibit a nearly complete set of repli-cation proteins. Reoxygenation triggers fast completion and post-translational modifications.
11p
tumor12
20-04-2013
31
2
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Antisense agents are valuable tools to inhibit the expression of a target gene in a sequence-specific manner,and may be used for functional genomics,target validation and thera-peuticpurposes.Three typesof anti-mRNAstrategies canbe distinguished. Firstly,the use of single stranded antisense-oligonucleotides; secondly,the triggering of RNA cleavage through catalytically active oligonucleotides referred to as ribozymes; and thirdly,RNA interference induced by small interfering RNA molecules.
17p
fptmusic
16-04-2013
42
2
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Mucin type O-glycosylation is a widespread modification of eukaryotic pro-teins. The transfer of N-acetylgalactosamine to selected serine or threonine residues is catalyzed by a family of polypeptide N-acetylgalactosaminyl-transferases localized in the Golgi apparatus. The most abundant elonga-tion of O-glycans is the addition of a b1-3 linked galactose by the core-1 b1-3 galactosyltransferase (core-1b3GalT), thereby building the T-antigen or core-1 structure Gal(b1-3)GalNAc(a1-O).
11p
fptmusic
11-04-2013
35
4
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We have investigated the molecular mechanisms that produce different structural and functional behavior in the monomeric and trimeric forms of seminal vesicle protein no. 4, a protein with immunomodulatory, anti-inflamma-tory, and procoagulant activity secreted from the rat seminal vesicle epithelium. The monomeric and trimeric forms were characterized in solution by CD.
9p
dell39
03-04-2013
35
5
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UDP-galactose 4-epimerases from the yeastKluyvero-myces fragilisandEscherichia coliare both homodimers but the molecular mass of the former (75 kDa/subunit) is nearly double that of the latter (39kDa/subunit). Protein databank sequence homology revealed the possibility of mutarotase activity in the excess mass of the yeast enzyme. This was confirmed by three independent assay protocols. With the help of specific inhibitors and chem-ical modification reagents, the catalytic sites of epimerase and mutarotase were shown to be distinct and inde-pendent....
11p
dell39
03-04-2013
44
4
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High-quality quantitative data generated under standardized conditions is critical for understanding dynamic cellular processes. We report strategies for error reduction, and algorithms for automated data processing and for establishing the widely used techniques of immunoprecipitation and immu-noblotting as highly precise methods for the quantification of protein levels and modifications.
12p
dell39
27-03-2013
54
3
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Murine Atg8L⁄Apg8L has significant homology with the other known mammalian Atg8 homologs, LC3, GABARAP and GATE-16. However, it is unclear whether murine Atg8L modification is mediated by human Atg4B, Atg7 and Atg3. Expression of Atg8L in HEK293 cells led to clea-vage of its C-terminus.In vitro, the C-terminus of Atg8L was cleaved by human Atg4B, but not human Atg4A or Atg4C.
10p
inspiron33
26-03-2013
40
5
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Protein glycation by methylglyoxal is a nonenzymatic post-translational modification whereby arginine and lysine side chains form a chemically heterogeneous group of advanced glycation end-products. Methylglyoxal-derived advanced glycation end-products are involved in pathologies such as diabetes and neurodegenerative diseases of the amyloid type.
15p
inspiron33
23-03-2013
52
4
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The crystal structure of human pancreatic cationic trypsin showed the chemical modification of Tyr154, which was originally described as phos-phorylation [Gaboriaud C, Serre L, Guy-Crotte O, Forest E & Fontecilla-Camps JC (1996)J Mol Biol259, 995–1010]. Here we report that Tyr154 is sulfated, not phosphorylated.
7p
inspiron33
23-03-2013
26
3
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Cellulose and wheat straw degradation byRuminococcus albuswas moni-tored using NMR spectroscopy. In situ solid-state 13 C-cross-polarization magic angle spinning NMR was used to monitor the modification of the composition and structure of cellulose and 13 C-enriched wheat straw during the growth of the bacterium on these substrates.
9p
galaxyss3
07-03-2013
40
3
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At the optimal temperature (65C),Thermus thermophiluspolynucleotide phosphorylase (Tth PNPase), produced inEscherichia colicells and isolated to functional homogeneity, completely destroys RNAs that possess even a very stable intramolecular secondary structure, but leaves intact RNAs whose 3¢ end is protected by chemical modification or by hybridization with a complementary oligonucleotide.
13p
media19
06-03-2013
46
3
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Peptides function as chemical signals between cells of multicellular organ-isms via specific receptors on target cells. Many hormones, neuromodula-tors and growth factors are peptides. Peptide hormones and other biologically active peptides are synthesized as higher molecular weight pre-cursor proteins (pro-hormones), which must undergo post-translational modification to yield the bioactive peptide(s).
16p
media19
06-03-2013
39
2
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Strategies for the chemical construction of synthetic proteins with precisely positioned post-translational modifications or their mimics offer a powerful method for dissecting the complexity of functional protein alteration and the associated complexity of proteomes.
11p
media19
06-03-2013
53
2
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Glycosylation is one of the most common post-translational modifications, and approximately 50% of all proteins are presumed to be glycosylated in eukaryotes. Branched N-glycans, such as bisecting GlcNAc,b-1,6-GlcNAc and core fucose (a-1,6-fucose), are enzymatic products of N-acetylglucos-aminyltransferase III,N-acetylglucosaminyltransferase V and a-1,6-fucosyl-transferase, respectively.
10p
media19
06-03-2013
32
4
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Free nucleotides in living cells play important roles in a variety of biolo-gical reactions, and often undergo chemical modifications of their base moieties. As modified nucleotides may have deleterious effects on cells, they must be eliminated from intracellular nucleotide pools.
13p
vinaphone15
27-02-2013
34
3
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